Diagnosis trajectories of prior multi-morbidity predict sepsis mortality

被引:67
作者
Beck, Mette K. [1 ,2 ]
Jensen, Anders Boeck [2 ]
Nielsen, Annelaura Bach [2 ]
Perner, Anders [3 ]
Moseley, Pope L. [2 ,4 ,5 ]
Brunak, Soren [2 ]
机构
[1] Tech Univ Denmark, Dept Syst Biol, Ctr Biol Sequence Anal, DK-2800 Lyngby, Denmark
[2] Univ Copenhagen, Novo Nordisk Fdn Ctr Prot Res, DK-2200 Copenhagen, Denmark
[3] Univ Copenhagen, Rigshosp, Dept Intens Care, DK-2100 Copenhagen, Denmark
[4] Univ Arkansas Med Sci, Coll Med, Dept Med, Little Rock, AR 72205 USA
[5] Univ Arkansas Med Sci, Coll Med, Dept Biomed Informat, Little Rock, AR 72205 USA
关键词
INTENSIVE-CARE-UNIT; ACUTE PHYSIOLOGY; CLASSIFICATION;
D O I
10.1038/srep36624
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Sepsis affects millions of people every year, many of whom will die. In contrast to current survival prediction models for sepsis patients that primarily are based on data from within-admission clinical measurements (e.g. vital parameters and blood values), we aim for using the full disease history to predict sepsis mortality. We benefit from data in electronic medical records covering all hospital encounters in Denmark from 1996 to 2014. This data set included 6.6 million patients of whom almost 120,000 were diagnosed with the ICD-10 code: A41 'Other sepsis'. Interestingly, patients following recurrent trajectories of time-ordered co-morbidities had significantly increased sepsis mortality compared to those who did not follow a trajectory. We identified trajectories which significantly altered sepsis mortality, and found three major starting points in a combined temporal sepsis network: Alcohol abuse, Diabetes and Cardio-vascular diagnoses. Many cancers also increased sepsis mortality. Using the trajectory based stratification model we explain contradictory reports in relation to diabetes that recently have appeared in the literature. Finally, we compared the predictive power using 18.5 years of disease history to scoring based on within-admission clinical measurements emphasizing the value of long term data in novel patient scores that combine the two types of data.
引用
收藏
页数:9
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